Solvent composition and water-repellent/oil-repellent composition using the same

ABSTRACT

A non-flammable water-repellent/oil repellent composition containing a fluorine containing-polymer and a solvent containing at least 40% by weight of a non-flammable perfluoro organic compound.

This application is a division, of application Ser. No. 08/487,673 filed Jun. 7, 1995, now abandoned; which, in turn, is a continuation of application Ser. No. 08/371,213, filed Jan. 11, 1995, now U.S. Pat. No. 5,458,692; which is a division of application Ser. No. 07/956,076, filed Oct. 2, 1992, now U.S. Pat. No. 5,403,514.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a novel nonflammable solvent composition having excellent characteristics as a solvent which can take the place of 1,1,2-trichloro-1,2,2-trifluoroethane (hereinafter abbreviated to "CFC-113"), and furthermore, it relates to a fluorine-based water-repellent/oil-repellent composition using the above-mentioned solvent composition and having water-repellent/oil-repellent properties, lubricating properties, mold release properties and the like.

2. Related Background Art

Most of chlorofluorocarbons (hereinafter abbreviated to "CFCs") are less toxic, incombustible and chemically stable, and various kinds of CFCs having different boiling points are available and therefore they have been utilized in many industrial fields. Above all, CFC-113 has been used as a degreasing solvent, a dispersant and a diluting solvent for a plastic material, a part of rubber materials and various composite materials by the utilization of its specific chemical characteristics.

In recent years, ozone holes which are due to unusual changes of earth environment have been discovered, and it has been elucidated that its main cause is organic chlorine-based compounds. Particularly chemically stable CFC-113 has a long life in the troposphere, and it diffuses and reaches the stratosphere. In the stratosphere, CFC-113 gives rise to photolysis under the influence of sunbeams to generate chlorine radicals. The thus generated chlorine radicals combine with ozone, so that an ozone layer is broken. Accordingly, the use of the organic chlorine-based compounds inclusive of the CFCs will be globally restricted and forbidden in the future. Among others, CFC-113 has a high ozone destruction coefficient, and hence its prompt replacement is desired and a severe schedule of reducing the employment of CFC-113 is justified.

SUMMARY OF THE INVENTION

An object of the present invention is to provide a novel solvent composition replaceable with CFC-113 which has been heretofore used in such circumstances.

Another object of the present invention is to provide a solvent composition suitable as a degreasing solvent for various substrates.

Still another object of the present invention is to provide a water-repellent/oil-repellent composition suitable as a modifier for the surfaces of various substrates.

The present invention for achieving the above-mentioned objects is directed to a nonflammable solvent composition containing 40% by volume or more of non-flammable perfluoro organic compound, and a nonflammable water-repellent/oil-repellent composition containing a fluorine-containing polymer and a solvent containing 40% by weight or more of a non-flammable perfluoro organic compound.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

The reasons why CFC-113 has often been used as a degreasing solvent are

(a) that it has a suitable solubility to various soils and oils,

(b) that it is excellent in chemical stability, and there is no worry of decomposition and the like,

(c) that it is less toxic and has neither a flash point nor an ignition point, and thus its operational safety is high, and

(d) that its polarity is low and it does not damage various plastic materials.

Therefore, in order to take the place of this CFC-113, similar characteristics are required. Nowadays, as the hydrochlorofluorocarbon (HCFC), there have been developed hydrochlorofluorocarbons such as 1,1-dichloro-2,2,2-trifluoroethane (hereinafter abbreviated to "HCFC-123"), 1-fluoro-1,1-dichloroethane (hereinafter abbreviated to "HCFC-141b"), 1,1-dichloro-2,2,3,3,3-pentafluoropropane (hereinafter abbreviated to "HCFC-225ca") and 1,3-dichloro-1,1,2,2,3-pentafluoropropane (hereinafter abbreviated to "HCFC-225cb"), and their substitution has been investigated.

However, most of these hydrochlorofluorocarbons have high solubility to various oils and fats but tend to attack substrates, particularly, general-purpose plastics such as acrylic resins and ABS resins, and therefore they are not considered to be all-round substitutes of CFC-113.

In order to satisfy the above-mentioned necessary properties, much attention is paid to perfluoro organic compounds having less chemical attack properties, and various kinds of solvent compositions have been intensively investigated. As a result, the present invention has been attained. That is, the solvent composition which can be used in the present invention contains a non-flammable perfluoro organic compound which has an extremely low polarity and no degreasing ability and which does not damage various substrates at all. In view of requirements of having no flash point, having a high vapor pressure, having a high chemical stability and having a reduced chemical attack to various materials, there can be suitably used perfluoroalkanes, perfluorocycloalkanes, perfluoro ethers, perfluoro cycloethers and the like as the perfluoro organic compounds which are used in the present invention.

Furthermore, the perfluoro organic compounds which can be used in the present invention preferably have a vapor pressure of 30 Torr or more at 250° C.

Typical examples of the perfluoro organic compounds include perfluoropentane (C₅ F₁₂), perfluorohexane (C₆ F₁₄), perfluoroheptane (C₇ F₁₆) perfluorooctane (C₈ F₁₈), perfluorocyclohexane (C₆ F₁₂), perfluorocycloheptane (C₇ F₁₄), perfluoro(alkylcyclohexane) (C₇ F₁₄ and C₈ F₁₆) and perfluoro(2-butyltetrahydrofuran) (C₈ F₁₆ O). The content of each of these perfluoro organic compounds is preferably 40% by volume or more based on the volume of the solvent composition of the present invention. When the content of the perfluoro organic compound is less than the above-mentioned amount, a flash point appears, and in the case that the compound is used in the form of a mixture with another flammable organic compound, the chemical attack of the flammable organic compound on products takes place inconveniently.

When the solvent composition of the present invention is used as the above-mentioned degreasing solvent, an organic compound having a degreasing power, particularly a flammable organic compound is added to the solvent composition.

This flammable organic compound having the degreasing power is required

(1) to be miscible with the perfluoro organic compound,

(2) to have a suitable dissolving power (the degreasing power) to various soils and oils, and

(3) to have a reduced chemical attack to products (particularly general-purpose plastics).

Examples of the particularly preferable organic compound which can meet the above-mentioned requirements include ether compounds, alkanes and cycloalkanes.

Preferable typical examples of the ether compounds include compounds represented by the formula

    R.sub.1 --O--R.sub.2

wherein R₁ is C_(n) H_(2n+1) or --Si(CH₃)₃, R₂ is C_(n) H_(2n+1) or --Si(CH₃)₃, and n and m meet 1≦n, m ≦4, and 2≦n+m≦6.

Preferable typical examples of the alkanes and cycloalkanes include compounds represented by the formulae

    C.sub.p H.sub.2p+2 and C.sub.q H.sub.2q

wherein p and q meet 5≦p and q≦8.

In order to satisfy the above-mentioned requirements (2) and (3), a particularly preferable embodiment is to use an organic compound having a solubility parameter (an SP value) of 7.5 or less. The SP values can be directly calculated from evaporation latent heat or vapor pressure, but in this specification, literature values mentioned in POLYMER HANDBOOK, 2nd Edition are employed and they are as follows (the values in parentheses were calculated in accordance with an intermolecular attraction constant method of Small). Preferable typical examples of such organic compounds are as follows:

    ______________________________________     n-pentane            SP value =                                   7.0                                   (7.2)     n-hexane             SP value =                                   7.3                                   (7.3)     2-methylpentane (isohexane)                          SP value =                                   (7.1)     2-methylhexane (isoheptane)                          SP value =                                   (7.2)     2,2,4-trimethylpentane (isooctane)                          SP value =                                   (6.8)     hexamethyldisiloxane (C.sub.8 H.sub.18 OSi.sub.2)                          SP =     (6.0)     diethyl ether (C.sub.4 H.sub.10 O)                          SP =     7.4 (7.3)     diisopropyl ether (C.sub.6 H.sub.14 O)                          SP =     7.0 (6.9)     methyl tert-butyl ether (C.sub.5 H.sub.12 O)                          SP =     (7.2).     ______________________________________

Furthermore, the solvent composition of the present invention can be also suitably used as a solvent composition for a water-repellent/oil-repellent agent which can modify the surfaces of substrates, i.e., can protect the substrates from contamination and impart water-repellent/oil-repellent properties to them.

As the solvent for the water-repellent/oil-repellent agent, 1,1,2-trichloro-1,2,2-trifluoroethane (CFC-113) has been overwhelmingly used for the reasons of the solubility of a polymer, safety, stability and the like. As other examples of the solvent, there have been used toluene, ethyl acetate and 1,1,1-trichloroethane, but these solvents tend to damage the substrates to be treated. Therefore, restriction is put on the selection of the substrates. In addition, most of these solvents are flammable, and therefore safety and the like are insufficient.

According to the present invention, there can be provided a non-ODC (Ozone Depletion Chemicals) type all-round water-repellent/oil-repellent composition which is free from a flash point and which is applicable to the various substrates without the restriction, by the use of a solvent composition containing 40% by weight or more of the above-mentioned non-flammable perfluoro organic compound as a solvent component of the water-repellent/oil-repellent composition.

In order to develop the non-ODC type all-round water-repellent/oil-repellent composition of the present invention which is applicable to the surfaces of the various substrates to be treated, a solute and a solvent are required to have the following characteristics.

Solute:

(a) To have a functional group for giving a sufficiently low surface energy, and

(b) to give a sufficient adhesive strength to the various substrates,

Solvent:

(a) To have selective solubility only to the solute, and neither to dissolve nor to swell other materials,

(b) to be less toxic, to have neither a flash point nor an ignition point, and thus to have high operational safety, and

(c) to have a high vapor pressure and a high drying rate.

For the purpose of obtaining the water-repellent/oil repellent composition which can meet all of the above-mentioned necessary characteristics, solvent mixtures have been intensively investigated, and as a result, the present invention has been attained.

The solute of the water-repellent/oil repellent composition which is used in the present invention is preferably a fluorine-containing polymer having a long-chain perfluoroalkyl group of C₆ F₁₃ or more as a functional group, and the polymer preferably contains 40 mole % or more of the fluorine-containing vinyl monomer so as to be highly fluorinated. The perfluoroalkyl group of C₆ F₁₃ or more as the functional group is particularly excellent in oil-repellency. In addition, also in the case that the polymer contains 40 mole % or more of the fluorine-containing vinyl monomer, the polymer is particularly excellent in oil-repellency. Typical examples of the solute which can be used in the present invention are as follows.

Homopolymer of 2-(perfluorooctyl)ethyl acrylate, homopolymer of (perfluoroheptyl)methyl methacrylate, homopolymer of 2-(N-ethylperfluorooctasulfoamido)ethyl acrylate, 2-(perfluorohexyl)ethyl methacrylate (60 mole % )/methyl methacrylate (30 mole % )/2-hydroxyethyl methacrylate (10 moles) copolymer, 2-(perfluorooctyl)ethyl acrylate (70 moles)/benzyl methacrylate (25 mole % )/2-hydroxyethyl methacrylate (5 mole % ) copolymer, and 2-(perfluoroisononyl)ethyl acrylate (50 mole % )/vinyl acetate (30 mole % )/methyl methacrylate (10 mole % )/2-hydroxyethyl methacrylate (10 mole % ) 1copolymer.

When it is desired to obtain the uniform and flat film, each of the above-mentioned solutes is preferably used in the range of from 0.01% to 5% by weight, more preferably in the range of from 0.05% to 1% by weight, based on the weight of the total components. A solute concentration of 0.01% by weight or more is particularly preferable in that the film having the sufficient oil-repellency can be formed, and at a solute concentration of 5% by weight or less, the uniform film can be obtained due to the solvation of the solute.

Furthermore, as the solvent composition for dissolving the above-mentioned solute which can be used in the water-repellent/oil-repellent composition of the present invention, a solvent for extinguishing a flash point of the total water-repellent/oil-repellent composition of the present invention and for relieving the damage to the substrate is preferable. In fact, the above-mentioned solvent composition of the present invention is suitable. In addition, usual organic solvents and chlorine-based solvents can be also used together with the solvent composition, depending upon kinds of solute and other additives.

Examples of the solvent which can be used together with the solvent composition of the present invention include fluorine-containing solvents, for example, perfluorocarboxylic acid derivatives such as methyltrifluoro acetate, ethyltrifluoro acetate and butylpentafluoro propionate; fluorine-based benzene derivatives such as hexafluorobenzene, pentafluorobenzene, benzotrifluoride and bistrifluoromethylbenzene; fluorine-containing alcohols such as trifluoroethanol, pentafluoropropanol and hexafluoroisopropanol; and hydrochlorofluorocarbons such as HCFC-123, HCFC-141b and HCFC-225.

Optional additives can be added to the water-repellent/oil-repellent composition of the present invention, so long as it has no flash point.

The water-repellent/oil-repellent composition of the present invention can be applied by the use of brush coating, immersion, spin coating, roll coating or spray coating.

EXAMPLES

Now, the present invention will be described in detail in reference to examples.

    ______________________________________     Example 1     Perfluorohexane         55 vol %     Diisopropyl ether       45 vol %     Example 2     Perfluoropentane        50 vol %     Diethyl ether           50 vol %     Example 3     Perfluoroheptane        60 vol %     Diisopropyl ether       40 vol %     Example 4     Perfluorohexane         25 vol %     Perfluoropentane        25 vol %     Isooctane               50 vol %     Example 5     Perfluorooctane         30 vol %     Perfluoro(butyltetrahydrofuran)                             20 vol %     Isooctane               50 vol %     Example 6     Perfluorohexane         60 vol %     Methyl tert-butyl ether 40 vol %     Example 7     Perfluorohexane         55 vol %     Isohexane               45 vol %     Example 8     Perfluorohexane         50 vol %     Hexamethyldisiloxane    50 vol %     Example 9     Perfluoropentane        20 vol %     Perfluorohexane         30 vol %     Methyl tert-butyl ether 25 vol %     n-hexane                25 vol %     Example 10     Perfluoropentane        20 vol %     Perfluorohexane         20 vol %     Diisopropyl ether       20 vol %     Isooctane               40 vol %     Comparative Example 1     CFC-113     Comparative Example 2     CFC-123     Comparative Example 3     CFC-141b     Comparative Example 4     CFC-225ca               50 vol %     CFC-225cb               50 vol %     Comparative Example 5     Perfluorohexane         20 vol %     Diisopropyl ether       80 vol %     Comparative Example 6     Perfluorohexane         30 vol %     Diisopropyl ether       60 vol %     ______________________________________

In Table 1, there are comparably shown characteristics of the mixed solvent compositions in the above-mentioned ratios.

Plastic resistance

In order to confirm that bad influences such as dissolution and swelling to general-purpose plastics were not present, a swelling test was made. Test pieces of the used general plastics were as follows.

    ______________________________________     PMMA (acryl)      Delpet 80N (Asahi Chemical                       Industry Co., Ltd.)     PC (polycarbonate)                       Panlight 1225 (Teijin                       Chemical Industry                       Co., Ltd.)     ABS (acrylonitrile/buta                       Saikorak EX120 (Ube Saikon     diene/styrene copolymer)                       Co., Ltd.)     POM (polyacetal)  Juracon M90 (Polyplastic                       Co., Ltd.)     PS (polystyrene)  HT53 (Idemitsu                       Petrochemicals                       Co., Ltd.)     Urethane rubber   Mirakutran E585 (Nippon                       Mirakutran Co., Ltd.)     ______________________________________

The test was made by cutting each test material into test pieces having a size of 25×100, immersing them in each solvent composition of the above-mentioned examples and comparative examples for 1 hour, and then calculating weight changes after the immersion. The test pieces having a weight change of less than 0.1% by weight are represented by o, the test pieces of from 0.1% by weight to 1% by weight are represented by Δ, and the test pieces of 1% by weight or more are represented by x.

Flammability

The flammability was measured in accordance with JIS K2265 by the use of a tag sealing type automatic flash point test machine (ATG-4 type; Tanaka Science Instrument Co., Ltd.).

Degreasing Power

As model contaminants, there were selected a cutting oil (MC-W, Idemitsu Kousan Co., Ltd.) and an anticorrosive oil (Polybutene LV-7, Nippon Petrochemicals Co., Ltd.), and 10 μl of each oil were dropped on a slide glass (25×76×1) to prepare contaminated model products. Each model product was immersed in 50 ml of each solvent composition of the examples and the comparative examples, and then washed with at room temperature for 1 minute by means of an ultrasonic washing machine of 28 kHz and 100 W. After the model product was pulled up, a degreasing power was evaluated at a contact angle of pure water on the model product.

Drying time

10 μl of each solvent composition were dropped on a slide glass, and a time which was taken until a weight change was not observed any more was measured.

ODP

Ozone depletion potentials (ozone destruction coefficient).

                                      TABLE 1     __________________________________________________________________________                              Flash                                  Degreasing                                         Drying     Plastic Resistance       Point                                  Power  Time     PMMA      PC                 ABS                    POM                       PS                         Urethane                               °C.!                                  MC-W                                      LV-7                                          sec!                                             ODP     __________________________________________________________________________     Example 1           ∘               ∘                 ∘                    ∘                       ∘                         ∘                              None                                  38  43  7  Absent     Example 2           ∘               ∘                 ∘                    ∘                       ∘                         ∘                              None                                  36  41 -2  Absent     Example 3           ∘               ∘                 ∘                    ∘                       ∘                         ∘                              None                                  39  44 19  Absent     Example 4           ∘               ∘                 ∘                    ∘                       ∘                         ∘                              None                                  36  42 20  Absent     Example 5           ∘               ∘                 ∘                    ∘                       ∘                         ∘                              None                                  36  41 50  Absent     Example 6           ∘               ∘                 ∘                    ∘                       ∘                         ∘                              None                                  37  43  7  Absent     Example 7           ∘               ∘                 ∘                    ∘                       ∘                         ∘                              None                                  35  40  6  Absent     Example 8           ∘               ∘                 ∘                    ∘                       ∘                         ∘                              None                                  39  45 22  Absent     Example 9           ∘               ∘                 ∘                    ∘                       ∘                         ∘                              None                                  36  41  7  Absent     Example 10           ∘               ∘                 ∘                    ∘                       ∘                         ∘                              None                                  35  41 15  Absent     Comp. Ex. 1           ∘               ∘                 ∘                    ∘                       ∘                         ∘                              None                                  36  41 28  Present     Comp. Ex. 2           x   x x  x  x x    None                                  35  40 10  Present     Comp. Ex. 3           x   x x  x  x x    None                                  36  41 10  Present     Comp. Ex. 4           x   ∘                 Δ                    ∘                       ∘                         x    None                                  36  42 31  Present     Comp. Ex. 5           ∘               ∘                 ∘                    ∘                       ∘                         ∘                              10  35  40  7  Absent     Comp. Ex. 6           ∘               ∘                 ∘                    ∘                       ∘                         ∘                              20  37  41  8  Absent     __________________________________________________________________________

    ______________________________________     Example 11     2-(perfluorooctyl)ethyl acrylate                           0.1%    by weight     (70 mole%)/benzyl methacrylate     (25 mole%)/2-hydroxyethyl     methacrylate (5 mole %)     copolymer     Perfluorohexane       90%     by weight (*)     Bistrifluoromethylbenzene                           9.9%    by weight     Note(*): This amount exceeds 40% by volume.     Example 12     Homopolymer of 2-(N-ethyl                           0.25%   by weight     per-fluoro octasulfoamide)ethyl     acrylate     Perfluoroheptane      99.75%  by weight (*)     Note(*): This amount exceeds 40% by volume.     Example 13     2-(perfluoroisononyl) ethyl                           1%      by weight     acrylate (50 mole %)/vinyl acetate     (30 mole %)/methyl methacrylate     (10 mole %)/2-hydroxyethyl     methacrylate (10 mole %)     copolymer     Perfluorohexane       50%     by weight (*)     Perfluoro-2-          40%     by weight (*)     butyltetrahydrofuran     Pentafluorobenzene    9%      by weight     Note(*): Sum of these amounts exceeds 40%     by volume.     Example 14     Homopolymer of        0.15%   by weight     (perfluorohexyl)-ethyl     acrylate     Perfluorohexane       60%     by weight (*)     Perfluoroheptane      20%     by weight (*)     Perfluorooctane       10%     by weight     Benzotrifluoride      9.85%   by weight     Note(*): Sum of these amounts exceeds 40%     by volume.     Example 15     (Perfluoroalkyl**) ethyl                           0.3%    by weight     acrylate (60 mole %)/methyl     methacrylate (30 mole %)/     hydroxyethylmethacrylate (10 moles)     copolymer     (**The perfluoroalkyl group was a mixture of     C.sub.4 F.sub.9 to C.sub.10 F.sub.21, and C.sub.8 F.sub.17 was the     main component.)     Perfluorooctane       45%     by weight (*)     Perfluoro-2-          45%     by weight (*)     butyltetrahydrofuran     Bistrifluoromethylbenzene                           9.7%    by weight     Note(*): Sum of these amounts exceeds 40%     by volume.     Comparative Example 7     2-(perfluorooctyl)ethyl                           0.1%    by weight     acrylate (70 mole %)/benzyl     methacrylate (25 mole %)/     2-hydroxyethylmethacrylate (5 mole %)     copolymer     CFC-113               99.9%   by weight     Comparative Example 8     2-(perfluorooctyl)ethyl                           0.1%    by weight     acrylate (70 mole %)/benzyl     methacrylate (25 mole %)/     2-hydroxyethylmethacrylate     (5 mole %) copolymer     CFC-113               90%     by weight     CFC-112               9.9%    by weight     Comparative Example 9     2-(perfluoroisononyl)ethyl                           1%      by weight     acrylate (50 mole %)/vinyl acetate     (30 mole %)/methyl methacrylate (10     mole %)/2-hydroxyethyl methacrylate     (10 mole %) copolymer     HCFC-225              99%     by weight     Comparative Example 10     2-(perfluoroisononyl) 1%      by weight     ethyl acrylate (50 mole %)/vinyl     acetate (30 mole %)/methyl     methacrylate (10 mole %)/2-     hydroxyethyl methacrylate     (10 mole %) copolymer     Pentafluoro propanol  99%     by weight     Comparative Example 11     (Perfluoroalkyl**)ethyl                           0.3%    by weight     acrylate (60 mole %)/methyl     methacrylate (30 mole %)/     hydroxyethyl methacrylate     (10 mole %) copolymer     (**The perfluoroalkyl group was a mixture of     from C.sub.4 F.sub.9 to C.sub.10 F.sub.21, and C.sub.8 F.sub.17 was the     main component.)     Ethyltrifluoro acetate                           60%     by weight     Perfluorohexane       39.7%   by weight (*)     Note(*): This amount does not exceed 40%     by volume.     Comparative Example 12     (Perfluoroalkyl**)ethyl                           0.3%    by weight     acrylate (60 mole %)/methyl     methacrylate (30 mole %)/     hydroxyethyl methacrylate     (10 mole %) copolymer     (**The perfluoroalkyl group was a mixture of     from C.sub.4 F.sub.9 to C.sub.10 F.sub.21, and C.sub.8 F.sub.17 was the     main component.)     HCFC-123              50%     by weight     HCFC-141b             49.7%   by weight     ______________________________________

In Table 2, there are comparably shown characteristics of the oil-repellent compositions in the above-mentioned ratios.

Evaluation of oil-repellency

Each oil-repellent composition was applied onto an acrylic substrate (Delpet 80N; Asahi Chemical Industry Co., Ltd.), and the oil-repellency was then evaluated at a contact angle by hexadecane.

Plastic resistance

In order to confirm that bad influences such as dissolution and swelling to general-purpose plastics were not present, a swelling test was made. As substrate materials to be used, there were selected PMMA (acryl), Delpet 80N (Asahi Chemical Industry Co., Ltd.), PC (polycarbonate), Panlight 1225 (Teijin Chemical Industry Co., Ltd.), ABS (acrylonitrile/butadiene/styrene copolymer), Saikorak EX120 (Ube Saikon Co., Ltd.), POM (polyacetal), Juracon M90 (Polyplastic Co., Ltd.), Urethane rubber, Mirakutran E585 (Nippon Mirakutran Co., Ltd.) and natural rubber. Each substrate having a size of 25×100×3 was immersed in each oil-repellent composition for 1 hour, and weight changes after the immersion were then calculated. The substrates having a weight change of less than 0.1% by weight are represented by o, the substrates of from 0.1% by weight to 1% by weight are represented by Δ, and the substrates of 1% by weight or more are represented by x.

Flammability

The flammability was measured in accordance with JIS K2265 by the use of a tag sealing type automatic flash point test machine (ATG-4 type: Tanaka Science Instrument Co., Ltd.).

Drying time 10 μl of each solvent composition were dropped on a slide glass, and a time which was taken until weight change was not observed any more was measured.

                                      TABLE 2     __________________________________________________________________________            Plastic Resistance Oil-  Water-                                           Flash                                               Drying                       Rubber                           Rubber                               Repellency                                     Repellency                                           Point                                               Time                                                   ODP            Acryl               PC                 ABS                    POM                       A   B    °C.!                                      °C.!                                            °C.!                                                sec!                                                   *1     __________________________________________________________________________     Example 11            ∘               ∘                 ∘                    ∘                       ∘                           ∘                               78    119   None                                               20  Absent     Example 12            ∘               ∘                 ∘                    ∘                       ∘                           ∘                               72    116   None                                               50  Absent     Example 13            ∘               ∘                 ∘                    ∘                       ∘                           ∘                               74    116   None                                               25  Absent     Example 14            ∘               ∘                 ∘                    ∘                       ∘                           ∘                               69    116   None                                               25  Absent     Example 15            ∘               ∘                 ∘                    ∘                       ∘                           ∘                               75    117   None                                               30  Absent     Comp. Ex. 7            ∘               ∘                 ∘                    Δ                       Δ                           x   77    118   None                                               28  Present     Comp. Ex. 8            ∘               ∘                 ∘                    Δ                       Δ                           x   77    117   None                                               30  Present     Comp. Ex. 9            x  ∘                 ∘                    ∘                       x   Δ                               74    116   None                                               31  Absent     Comp. Ex. 10            x  x x  ∘                       Δ                           Δ                               73    115   None                                               90  Absent     Comp. Ex. 11            Δ               Δ                 Δ                    Δ                       Δ                           Δ                               72    116   25  75  Absent     Comp. Ex. 12            x  x x  x  x   x   73    116   None                                               10  Present     __________________________________________________________________________      Rubber A: Urethane rubber      Rubber B: Natural rubber      *1: ODP: Ozone depletion potentials (ozone destruction coefficient) 

What is claimed is:
 1. A method for modifying a surface of a substrate comprising: applying to the substrate a non-flammable water-repellent/oil repellent composition consisting essentially of a 0.01 to 5.0% by weight of fluorine-containing polymer and a solvent composition comprising a non-flammable perfluoro organic compound in an amount of not less than 40% by weight, thereby forming a film consisting of fluorine-containing polymer on the surface of the substrate.
 2. The method according to claim 1, wherein said perfluoro organic compound is a compound having a vapor pressure of 30 Torr or more at 25° C.
 3. The method according to claim 1, wherein said fluorine-containing polymer contains 40 mole % or more of a monomer of a fluorine-containing vinyl compound selected from the group consisting of fluoroalkyl acrylate, fluoroalkyl methacrylate and fluoroalkyl vinyl ether.
 4. The method according to claim 1, wherein said fluorine-containing polymer is a polymer which comprises a monomer containing a perfluoroalkyl group having a molecular weight more than C₈ F₁₃.
 5. The method according to claim 1, wherein said perfluoro organic compound is at least one selected from the group consisting of perfluoroalkanes, perfluorocycloalkanes and perfluoro cyclic ethers.
 6. The method according to claim 5, wherein said perfluoroalkanes and perfluorocycloalkanes are selected from the group consisting of C₅ F₁₂, C₆ F₁₄, C₇ F₁₆, C₈ F₁₈, C₆ F₁₂, C₇ F₁₄ and C₈ F₁₆.
 7. The method according to claim 5, wherein said perfluoro cyclic ethers are selected from the group consisting of C₆ F₁₂ O, C₇ F₁₄ O and C₈ F₁₆ O. 